Julia Robinson
Co-Founder/Vice President

Sickle Cell advocate. Julia has first-hand experience with Sickle Cell Disease after losing a warrior to Sickle Cell Disease 2014.

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Thank you for reaching out to Robinson's Sickle Cell Foundation: HOLD a HEART! If you or someone you know is living with SCD and could benefit from our services, or if you have any questions or comments, please don't hesitate to contact us using the form below. We will do our best to get back to you as soon as possible.